A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15673554



Internal ID5675370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38807222..38808684hg38UCSC Ensembl
Innerchr17:38807225..38808682hg38UCSC Ensembl
Outerchr17:38807220..38808687hg38UCSC Ensembl
chr17:36963475..36964937hg19UCSC Ensembl
Innerchr17:36963478..36964935hg19UCSC Ensembl
Outerchr17:36963473..36964940hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381463
hg191463
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640530
Supporting Variants
SamplesHG02419
Known GenesCWC25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15673554
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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